US2014484A - Azo dyestuffs - Google Patents

Description

Patented Sept. 17, 1935 UNITED STATES PATENT OFFEQE AZO DYE STUFFS Richard Stiisser, Cologne-Deutz, Karl Dobmaier, Leverkusen, and Richard Stroebel, Dusseldorf, Germany, assignors to General Aniline Works, 1110., New York, N. Y., a corporation of Delaware No Drawing.

Application December 30, 1931,

Serial No. 584,014. In Germany January 10,

4 Claims. (Cl. 260-'78) wherein R stands for the radical of a diazotization component of the benzene or naphthalene series containing a substituent of the group consisting of hydroxyl and carboxylic acid group which substituent stands in ortho-position to the azo groupattached to the radical R in accordance with the above formula, which R, may be further substituted by a sulfonic acid group, a nitro group, alkyl,

alkoxy, halogen and the group N=N-R', in which R means the same as defined hereafter, R stands for a radical of a hydroxyor an aminocarbazole compound capable of being coupled to form an azo dyestufi, that means a carbazole being substituted at least by a hydroxyor/ and an amino-group and having a free position in orthoposition to the hydroxy or amino group, R may be further substituted by a sulfonic acid group, a carboxylic acid group, alkyl and the group N:NR., in which R means the same as stated above, the substituents -N=NR. and --N: NR not being simultaneously present in the molecule.

We wish it to be understood that the mononuclear aromatic amines of the benzene series as well as diphenyl compounds, such as benzidine derivatives or other diaminodiphenyl compounds in which the phenyl nuclei are linked together by a bridge such as a sulfone bridge, a urea bridge or an azo group fall within the scope of the definition of the figure R of the above formula.

Our new dyestuffs are obtainable in the usual manner of preparing azo dyestuffs by diazotizing or tetrazotizing an aromatic amine of the benzene or naphthalene series or by diazotizing an amino azo compound and coupling with the coupling components referred to above. The various methods of synthesizing our new dyestuffs more fully are described in the following examples.

The new dyestuffs generally are dark powders dyeing brown to blackish violet shades; the dyestuffs containing a sulfonic or carboxylic acid group are in the form of their alkali metal salts 50 water soluble dark powders, dyeing the fibre brown to blackish violet shades which by after-treatment with a suitable heavy metal compound, especially a copper, chromium or cobalt compound, become very fast to light. The heavy metal complex 55 compounds of our new dyestuffs prepared in substance partially are valuable for dyeing leather.

We Wish it to be understood that both the dyestuffs free from the heavy metal as well as the heavy metal complex compounds are included within the scope of our invention. 5

' The following examples illustrate the invention without limiting it thereto Example 1.224 parts by weight of 6-chlorol-hydroxy-Z-amino benzenei-sulfcnic acid are diazotized in the usual manner with 69 parts by 10 weight of sodium nitrite and 350 parts by weight of hydrochloric acid of 19 B. and coupled in alkaline solution with 198 parts by weight of 2- hydroxy-3-aminocarbazo1e. The coupling may be accelerated by the addition of a small quantity of 15 pyridine. When the coupling is complete, the dyestuff, having in its free state the following formula:

Cl OH OH IITH: 20

OzN OH on 40 l S 0 3H HN/ dyeing wool brown shades which by after-chroming become violet, by after cobalting red very fast to light.

Example 3.--Analogously to the process described in Example 1 there is obtained from 1 mol of diazotized 6-nitro-2-amino-l-hydroxybenzenel-sulfonic acid and 1 mol of Z-amino- 55 carbazole a dyestuif dyeing wool, when after chromed, brownish black shades fast to milling and potting.

Example 4.-An-alogously to the process described in Example 1 there is obtained from 1 mol of diazotized 6-chloro-2-amino-1-hydroxybenzene--sulfonic acid and 1 mol of 2-hydroxycarbazole a dyestuff dyeing wool, when after chromed, violet shades.

By substituting the 2-hydroxycarbazole by the 2-hydroxycarbazole-3-carboxylic acid, there is obtained a dyestuff yielding, when after chromed violet reddish-brown shades.

By substituting the 6-chloro-2amino-l-hydroxybenzene-4-sulfonic acid, by the 2-amino-lhydroxybenzene-l,6-disu1fonic acid there is obtained a dyestuif dyeing wool, when after chromed, reddish-violet shades.

Example 5. Analogously to the process described in Example 1 there is obtained from 1 mol of diazotized 4-chloro-2-amino-l-hydroxybenzene-G-sulfonic acid and 1 mol of 9-methyl-2-hydroxycarbazole a dyestuff dyeing wool, when after chromed violet shades.

Example 6.-Analogously to the process described in Example 1 there is obtained from 2 mols of 4-nitro-2-amino-l-hydroxybenzene and 1 mol of 1,8-dihydroxycarbazole-3,6-disulfonic acid a dyestuff having in its free state the following formula:-

IITOz HO S S0311 Non I I I I 6H OH H OH OH dyeing wool, when after chromed, reddish black shades of good fastness to carbonizing and potting.

By substituting the 4-nitro-2-amino-1-hydroxybenzene by 2 mols of 2-amino-benzoic acid there is obtained a dyestuif dyeing wool, when after chromed, reddish brown shades.

Example 7.Analogously to the process described in Example 1, there is obtained from 1 mol of diazotized 1-sulfo-2-aminobenzoic acid and 1 mol of 3-amino-Z-hydroxycarbazole a dyestufi dyeing wool, when after chromed, reddish violet shades.

Example 8.Analogously to the process described in Example 1, there is obtained from 1 mol of diazotized 5sulfo3-amino-2hydroxybenzoic acid and 1 mol of 2-hydroxycarbazole a dyestuff dyeing wool, when after chromed, yellowish brown shades.

Example 9.Analogously to the process described in Example 1, there is obtained from 1 mol of 5-nitro-3-amino-2-hydroxybenzoic acid and 1 mol of l-hydroxycarbazole-3.S-disulfonic acid a dyestuff having in its free state the following formula:

IIIO HOaS- SOaH I NH 13000 (I)H bazole and 1 mol of resorcin there is obtained a dyestuff having in its free state the following formula dyeing the vegetable fibre, when after treated with a copper compound yielding copper, reddish brown shades.

Example 11.Analogously to the process de- 15 scribed in Example 1, there is obtained from 1 mol of di-azotized 4-hydro-xy-3-amino-l-methylbenzene and 1 mol of 1.8-dihydroxycarbazole-3.6-disulfonic acid a dyestuff dyeing wool, when after chromed, a violet-tinged brown. 20

By substituting the 4-hydroxy-3-amino-1- methylbenzene by 1 mol of lA-dimethoxy-Z- amino-S-nitrobenzene, there is obtained a dyestuff dyeing wool when after chromed reddish brown shades.

Example 12.Analogously to the process described in Example 1, there is obtained from 1 mol of diazotized 5-sulfo-2-aminobenzoic acid and 1 mol of 2-hydroxycarbazole-3-earboxylic acid a dyestuff having in its free state the following 30 formula chroming a brownish red of good fastness properties is obtained.

By refluxing the dyestuff with the addition of chromium formate until the dyestufi is no more sensitive to acids and alkalies a complex chromium compound is obtained dyeing leather brown shades of excellent fastness to light.

Example 13.-By coupling 1 mol of diazotized 2-amino-1-hydroxybenzene-4-sulfonic acid with 1 mol of 1,2-benzocarbazole-3'-hydroxy-2'-carboxylic acid there is obtained a dyestuff having in its free state the following formula HOQIS NH ON=N 0 0 OH in aqueous sodium carbonate solution and boiling with the addition of ammoniacal copper sulfate solution, there is obtained a complex copper compound of the dyestuff dyeing leather 3, violet tinged black of good fastness to light.

The complex chromium compound of the dyestuff which is obtainable by boiling the same with chromium fluoride dyes leather greenish black shades of good fastness properties.

Example 14.-15.4 parts by weight of 4-nitro- 2-aminophenol are diazotized and added to an ice cold solution of 20.2 parts by weight of 2- hydroxycarbazole, dissolved in 500 parts by wherein R stands for the radical of a diazotizaweight of water with the addition of 4 parts by tion component of the benzene or naphthalene weight of caustic soda and 50 parts by weight series, x stands for a hydroxy or carboxylic acid of soda. The dyestuff separates, is sucked ofi group and R stands for the radical of a hydroxyand refluxed in 500 parts by weight of triethanolor an arnino-carbazole compound capable of be- 5 amine with the addition of 40 parts by weight of ing coupled to form an azo dyestuff, being gena chromium chloride solution of 50% strength erally dark powders dyeing brown to blackish until the dyestufi is no more sensitive to alkalies violet shades and yielding when after-treated and dilute acids. By the addition of water, the with a compound yielding a heavy metal of the dyestuff is precipitated and is sucked 01f after group consisting of copper, chromium and 00- 0O01ing. It is a dark powder Soluble in Organic halt the corresponding heavy metal complex solvents such as pyridine and is a valuable pigcompounds of th azo dyestuffs,

ment dyestuif. 2. The azo dyestufi of the following formula:

Example 15,-253 parts by weight of 5-n1troz-anisidinel-sulfonic acid are diazotized and in- 00011 CODE 03 troduced into an ice cold solution, prepared by dissolving 20.2 parts by weight of Z-hydroxycar- O C O bazole and 500 parts by weight of water with the addition of 4 parts by weight of caustic soda and OH EN 50 parts by weight of soda. The isolated dyestuff is transformed into its complex copper compound by refluxing for several hours in an ammoniacal solution prepared from 30 parts by W the Vegetable fibre, after-treated weight of copper sulfate. The copper compound Wlth copper compound Yleldmg copper,

hav'n in the free state robably the following dish brown Shadesfoflimglaz p 3. The azo dyestufi of the following formula:

- OzN on 011 0( .2 u 0 l l I HO G Q 502E HN N02 EN 2 dyeing wool brown shades which by after-chromis a brown water soluble powder, dyeing leather ing become violet, by after-cobalting red, very fawn-colored shades of good fastness to light. fast to light.

Example 16.-When tetrazotizing 1 mol of 4.4'- 4. The azo dyestuff of the following formula: diaminodiphenylurea-3.3-dicarboxylic acid and. successively coupling with 1 mol of l-hydroxyom H033 Sea 40 carb-azole-3.G-disulfonic acid and 1 mol of the pyrazolone of 2-aminonaphthalene-4.8-disulfonic N: acid, there is obtained a dyestuff having in its I 1 NH free state the following formula H000 OH OH on com 00:11 NH N=N-C NHO 0-NH N=N HOsS- SOaH Ho=s- The complex copper compound of this dyestufl dyeing wool, when after-chromed, reddish brown is a brown water soluble powder dyeing the cellushades.

lose fibre brown shades very fast to light. RICHARD STI J'SSER.

We claim:- KARL DOBMAIER. 1. A20 dyestuffs of the general formula: RICHARD 'STROEBEL.